C57BL/6NTac-Hellstm1a(EUCOMM)Wtsi/Ieg
Status | Available to order |
EMMA ID | EM:04583 |
International strain name | C57BL/6NTac-Hellstm1a(EUCOMM)Wtsi/Ieg |
Alternative name | EPD0102_4_A04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Hellstm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Hells |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0102_4_A04. For further details on the construction of this clone see the page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6NTacUSA, wild-type C57BL/6NTacUSA |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- ICF syndrome / Orphanet_2268
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- preweaning lethality, complete penetrance / IMPC
- dilated heart left ventricle / IMPC
- decreased heart rate / IMPC
- decreased circulating cholesterol level / IMPC
- decreased monocyte cell number / IMPC
- decreased circulating triglyceride level / IMPC
- increased cardiac stroke volume / IMPC
- abnormal gait / IMPC
- decreased circulating LDL cholesterol level / IMPC
- increased CD8-positive, alpha-beta T cell number / IMPC
MGI phenotypes (gene matching)
- delayed bone ossification / MGI
- decreased bone mineral density / MGI
- osteoporosis / MGI
- abnormal long bone epiphysis morphology / MGI
- kyphosis / MGI
- hypoglycemia / MGI
- decreased cell proliferation / MGI
- alopecia / MGI
- abnormal tibia morphology / MGI
- small spleen / MGI
- small thymus / MGI
- atelectasis / MGI
- hyperkeratosis / MGI
- decreased body weight / MGI
- abnormal gait / MGI
- thymus hypoplasia / MGI
- respiratory failure / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal axial skeleton morphology / MGI
- abnormal kidney morphology / MGI
- abnormal renal tubule morphology / MGI
- dilated renal tubules / MGI
- short tibia / MGI
- small kidney / MGI
- abnormal thoracic vertebrae morphology / MGI
- short femur / MGI
- paternal imprinting / MGI
- decreased cellular sensitivity to gamma-irradiation / MGI
- delayed endochondral bone ossification / MGI
- abnormal chromosome morphology / MGI
- abnormal long bone morphology / MGI
- premature aging / MGI
- abnormal chromosome number / MGI
- increased renal tubule apoptosis / MGI
- renal tubular necrosis / MGI
- abnormal proximal convoluted tubule morphology / MGI
- decreased B cell number / MGI
- increased double-negative T cell number / MGI
- cachexia / MGI
- increased CD8-positive, alpha-beta T cell number / MGI
- decreased subcutaneous adipose tissue amount / MGI
- decreased embryo weight / MGI
- decreased fetal weight / MGI
- decreased birth weight / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, complete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
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